Primary Device ID | 10810020083139 |
NIH Device Record Key | 48146faf-eee9-4afd-8ae7-eb37baa3fb9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Gold Marker |
Version Model Number | GM1033 |
Company DUNS | 964053560 |
Company Name | RIVERPOINT MEDICAL, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810020083132 [Primary] |
GS1 | 10810020083139 [Package] Contains: 00810020083132 Package: [10 Units] In Commercial Distribution |
NEU | Marker, Radiographic, Implantable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-03 |
Device Publish Date | 2020-03-26 |
10812444028826 | Gold Marker |
30812444027991 | GM1254 |
30812444027977 | Brachytherapy |
00812444027136 | BRACHYTHERAPY |
00812444025842 | BRACHYTHERAPY |
00812444024739 | BRACHYTHERAPY |
00812444024449 | BRACHYTHERAPY |
00812444023527 | BRACHYTHERAPY |
00812444023510 | BRACHYTHERAPY |
00812444023282 | BRACHYTHERAPY |
00812444023275 | BRACHYTHERAPY |
00812444022209 | Brachytherapy |
00812444022049 | SUTURE |
10810020083146 | Brachytherapy |
10810020083139 | Brachytherapy |